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Research 271–300 of 519
- The Rotterdam Study: objectives and design update
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- The JAK/STAT signaling pathway: from bench to clinic
- New aspects of vitamin D metabolism and action — addressing the skin as source and target
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Maintenance of Hair Follicle Immune Privilege Is Linked to Prevention of NK Cell Attack
- Vaccines, adjuvants and autoimmunity
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- The Rotterdam Study: 2010 objectives and design update
- Quiescent Tissue Stem Cells Evade Immune Surveillance
- Biotin and biotinidase deficiency
- WNT Signaling in Disease
- Autoimmunity: Alopecia Areata
- FGF5 is a crucial regulator of hair length in humans
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Recurrent implantation failure: A comprehensive summary from etiology to treatment
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Gene Array Profiling and Immunomodulation Studies Define a Cell-Mediated Immune Response Underlying the Pathogenesis of Alopecia Areata in a Mouse Model and Humans
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- The Role of Hair Follicle Immune Privilege Collapse in Alopecia Areata: Status and Perspectives
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Superior Root Hair Formation Confers Root Efficiency in Some, But Not All, Rice Genotypes upon P Deficiency